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Facilitative transporter

Facilitated transport membranes can be used to separate gases membrane transport is then driven by a difference in the gas partial pressure across the membrane. Metal ions can also be selectively transported across a membrane driven by a flow of hydrogen or hydroxyl ions in the other direction. This process is sometimes called coupled transport. [Pg.76]

Because the facilitated transport process employs a specific reactive carrier species, very high membrane selectivities can be achieved. These selectivities are often far higher than those achieved by other membrane processes. This one fact has maintained interest in facilitated transport since the 1970s, but the problems of the physical instability of the liquid membrane and the chemical instability of the carrier agent are yet to be overcome. [Pg.76]

Decaffeinated coffee products represented 18% of the coffee consumed in 1991 in the United States (31). Decaffeinated coffee was first developed commercially in Europe about 1900. The process as described in a 1908 patent (35) consists of first, moisturizing green coffee to at least 20% to facilitate transport of caffeine through the cell wall, and then contacting the moistened beans with solvents. [Pg.389]

Facilitated Transport Transport by a reacti -e phase through a membrane is promising but problematic. Way and Noble [in Ho and Sirkar (eds,), op, cit, pp, 833-866] haye a description and a complete bibliography. [Pg.2023]

Carriers and channels may be distinguished on the basis of their temperature dependence. Channels are comparatively insensitive to membrane phase transitions and show only a slight dependence of transport rate on temperature. Mobile carriers, on the other hand, function efficiently above a membrane phase transition, but only poorly below it. Consequently, mobile carrier systems often show dramatic increases in transport rate as the system is heated through its phase transition. Figure 10.39 displays the structures of several of these interesting molecules. As might be anticipated from the variety of structures represented here, these molecules associate with membranes and facilitate transport by different means. [Pg.321]

The discussion so far implies that membrane materials are organic polymers, and in fact most membranes used commercially are polymer-based. However, in recent years, interest in membranes made of less conventional materials has increased. Ceramic membranes, a special class of microporous membranes, are being used in ultrafiltration and microfiltration applications for which solvent resistance and thermal stability are required. Dense, metal membranes, particularly palladium membranes, are being considered for the separation of hydrogen from gas mixtures, and supported liquid films are being developed for carrier-facilitated transport processes. [Pg.353]

In PBPK models tissue blood perfusion and tissue composition can be characterized independently of the drug thus such a model can be created once and reused for many different drugs. Furthermore, because physical laws (mass conservation, diffusion, or facilitated transport mechanisms) are incor-... [Pg.539]

The Creatine Phosphate Shuttle Facilitates Transport of High-Energy Phosphate From Mitochondria... [Pg.100]

In the liver, the bilirubin is removed from albumin and taken up at the sinusoidal surface of the hepato-cytes by a carrier-mediated saturable system. This facilitated transport system has a very large capacity, so that even under pathologic conditions the system does not appear to be rate-limiting in the metabolism of bilirubin. [Pg.280]

Since this facilitated transport system allows the equilibrium of bilirubin across the sinusoidal membrane of the hepatocyte, the net uptake of bilirubin will be dependent upon the removal of bilirubin via subsequent metabolic pathways. [Pg.280]

Novel chiral. separations using enzymes and chiral surfactants as carriers have been realized using facilitated transport membranes. Japanese workers have reported the synthesis of a novel norbornadiene polymeric membrane with optically active pendent groups that show enantio.selectivity, which has shown promi.se in the. separation of propronalol. [Pg.430]

Absorption. No studies were located regarding the mechanism of absorption in humans or animals after inhalation, oral, or dermal exposure to diisopropyl methylphosphonate. Both facilitated transport and diffusion through the lipophilic portions of the membrane could be involved in absorption processes. No data were found regarding lipid solubility or partition coefficients. [Pg.75]

Facilitated transport combines some properties of both mechanisms discussed above. This type of transport is carrier mediated so that there is substrate specificity, a transport maximum, and competitive inhibition. However, facilitated transport is not energy-dependent and is unable to transport a substrate against a concentration gradient. [Pg.435]

A one-electron path, however, has been successfully used in conjunction with organometallic complexes, as used in facilitated transport (non-electrochemical... [Pg.213]

The mechanism of facilitated transport involves using the metal ion only in its reduced state in the oxidized state the oxygen-carrying capacity is virtually nil. It is thus natural that electrochemical processes should be attempted to improve both the flux and selectivity obtained with the membranes described above by exploiting this 02 capacity difference. For example, the best of the ultra-thin membranes developed by Johnson et al. [24] delivered oxygen at a rate equivalent to a current density of only 3 mA/cm2, at least an order lower than that achievable electrochemically. Further, the purity was but 85% and the lifetime of the carrier less than a year. [Pg.214]

Fig. 9. Facilitated transport of oxygen by a carrier in a liquid membrane. Fig. 9. Facilitated transport of oxygen by a carrier in a liquid membrane.
There seems to be an opportunity to extend the electrochemical process to direct membrane transport that is, with electrodes plated on either side of a facilitated-transport membrane similar to that of Johnson [24]. The shuttling action of the carrier (Fig. 9) could then be brought about by electrochemical reduction and oxidation instead of pressure difference. [Pg.219]

The basic mechanism for surfactants to enhance solubility and dissolution is the ability of surface-active molecules to aggregate and form micelles [35], While the mathematical models used to describe surfactant-enhanced dissolution may differ, they all incorporate micellar transport. The basic assumption underlying micelle-facilitated transport is that no enhanced dissolution takes place below the critical micelle concentration of the surfactant solution. This assumption is debatable, since surfactant molecules below the critical micelle concentration may improve the wetting of solids by reducing the surface energy. [Pg.140]

In addition to faster solute transport rates, the major experimental features of membrane-facilitated transport that distinguish it from membrane diffusion include (1) specificity and selectivity (2) saturability (3) inhibition, activation, and cooperativity (4) transmembrane effects and (5) greater temperature sensitivity than is characteristic of membrane diffusion [42],... [Pg.182]

Two distinguishing features of gastrointestinal active and facilitated transport processes are that they are capacity-limited and inhibitable. Passive transcellular solute flux is proportional to mucosal solute concentration (C), where the proportionality constant is the ratio of the product of membrane diffusion coefficient (Dm) and distribution coefficient (Kd) to the length of the transcellular pathway (Lm). [Pg.184]

Mass transport of the reactants and products is increased at the catalyst surface and in the solution due to the facilitated transport as a result of shockwave propagation. [Pg.59]


See other pages where Facilitative transporter is mentioned: [Pg.390]    [Pg.103]    [Pg.76]    [Pg.223]    [Pg.298]    [Pg.298]    [Pg.299]    [Pg.91]    [Pg.99]    [Pg.948]    [Pg.99]    [Pg.414]    [Pg.137]    [Pg.475]    [Pg.278]    [Pg.161]    [Pg.200]    [Pg.196]    [Pg.36]    [Pg.25]    [Pg.804]    [Pg.152]    [Pg.445]    [Pg.573]    [Pg.120]    [Pg.214]    [Pg.183]    [Pg.183]    [Pg.93]   
See also in sourсe #XX -- [ Pg.23 , Pg.26 , Pg.27 ]




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